dc.contributor.author | Kumar, Indresh | |
dc.date.accessioned | 2021-10-27T04:27:18Z | |
dc.date.available | 2021-10-27T04:27:18Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra04741g | |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3161 | |
dc.description.abstract | An efficient protocol for the synthesis of 2,2-disubstituted indolin-3-ones under mild conditions has been developed. This reaction involves the copper-catalyzed in situ oxidative de-aromatization of 2-arylindoles to indol-3-one, followed by self-dimerization as well as cross-addition with indoles under mild conditions. The result generates a wide variety of C2-tetrasubstituted indolin-3-ones with good to high yields (62–82%). | en_US |
dc.language.iso | en | en_US |
dc.publisher | RSC | en_US |
dc.subject | Chemistry | en_US |
dc.subject | C2-tetrasubstituted | en_US |
dc.subject | Indolin-3-ones | en_US |
dc.subject | Cu-catalyzed | en_US |
dc.title | Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles | en_US |
dc.type | Article | en_US |
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